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Antibody-modified microwell arrays and photobiotin patterning on hydrocarbon-free glass

机译:无烃玻璃上的抗体修饰微孔阵列和光生物素构图

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Antibody-modified microwell arrays were fabricated using site-selective photobiotin chemistry and the biotin-avidin interaction. In one scheme, an aminopropyl-functionalized glass surface was the starting substrate and in the other an acid-treated glass surface was employed. In both schemes, the substrates were coated with the aryl azide photobiotin, and photoactivated with ultraviolet radiation to afford biotin-modified arrays before sequential reactions with ExtrAvidin, biotinylated-IgG, and dye-labeled anti-IgG. Antibody-modified microwell arrays were characterized using fluorescence microscopy. In both schemes, the biotin-avidin-biotin linkage was stable, and there was negligible non-specific binding (NSB) of photobiotin, ExtrAvidin, and dye-labeled anti-IgG to the modified substrates. However, negligible NSB of biotinylated-IgG was observed only with the acid-treated glass surface. To further characterize the nitrene reactions on these hydrocarbon-free glass surfaces, we developed a new protocol using a fluorescent-labeled aryl azide in place of photobiotin. Fluorescence microscopy characterizations of these modified surfaces revealed that detectable fluorescence was observed only from silanol-rich, acid-treated glasses. It is believed this work represents the first demonstration of photo-initiated reactions of photobiotin with reactive silanols on acid-treated glass surfaces. (c) 2006 Elsevier B.V. All rights reserved.
机译:使用位点选择性光生物素化学和生物素-亲和素相互作用制备了抗体修饰的微孔阵列。在一种方案中,将氨基丙基官能化的玻璃表面作为起始基材,而在另一种方案中,采用酸处理的玻璃表面。在这两种方案中,在用ExtrAvidin,生物素化的IgG和染料标记的抗IgG进行顺序反应之前,用芳基叠氮化物光生物素包被基质,并用紫外线进行光活化,以提供生物素修饰的阵列。使用荧光显微镜表征了抗体修饰的微孔阵列。在这两种方案中,生物素-亲和素-生物素连接均稳定,并且光生物素,ExtrAvidin和染料标记的抗IgG与修饰底物的非特异性结合(NSB)可以忽略。然而,仅在酸处理的玻璃表面上观察到的生物素化IgG的NSB可以忽略不计。为了进一步表征这些无烃玻璃表面上的腈反应,我们开发了一种新的方案,使用荧光标记的芳基叠氮化物代替光生物素。这些改性表面的荧光显微镜检定表明,仅从富含硅烷醇的酸处理玻璃中观察到可检测到的荧光。相信这项工作代表了光生物素与酸处理的玻璃表面上反应性硅烷醇的光引发反应的首次证明。 (c)2006 Elsevier B.V.保留所有权利。

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